Publications by authors named "Ali Ahani"

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Whole-exome sequencing reveals a novel mutation in the gene causing acephalic spermatozoa syndrome.
Seyedeh-Hanieh Hosseini, Nastaran Salehisedeh, Mahsa Allahgholi, Ali Ahani, Mohammad Ali Sadighi Gilani

Reprod Fertil Dev· July 2025

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A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies.
Sareh Hosseinpour, Ehsan Razmara, Morteza Heidari, Zahra Rezaei, Mahmoud Reza Ashrafi, Ali Ahani

Brain Dev· April 2024

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Refractory Complex Regional Pain Syndrome: A Case Report and Review of Literature.
Mahmood-Reza Alebouyeh, Seyedeh Fatemeh Morsali, Faegheh Zojaji, Seyed Ali Ebrahimi, Ali Ahani

Anesth Pain Med· August 2023

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Erector Spinae Plane Block for the Treatment of Intractable Pain in a Patient with Pancoast Tumor: A Case Report.
Poupak Rahimzadeh, Ali Ahani, Ali Antar, Seyedeh Fatemeh Morsali, Faegheh Zojaji

Anesth Pain Med· June 2023

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Prevalence of human papilloma virus (HPV) genotypes between outpatients males and females referred to seven laboratories in Tehran, Iran.
Iman Rezaee Azhar, Mahmood Yaghoobi, Mir Majid Mossalaeie, Abolghasem Kollaee Darabi, Amir Houshang Nejadeh, Ali Ahani

Infect Agent Cancer· March 2022

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Identical twins with progressive kyphoscoliosis and ophthalmoplegia.
Maziar Emamikhah, Gholamali Shahidi, Elaheh Amini, Alfonso Fasano, Anthony E Lang, Ali Ahani

Parkinsonism Relat Disord· November 2021

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Recommendation agents and information sharing through social media for coronavirus outbreak.
Mehrbakhsh Nilashi, Shahla Asadi, Behrouz Minaei-Bidgoli, Rabab Ali Abumalloh, Sarminah Samad, Ali Ahani

Telemat Inform· August 2021

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The Association between TNF-alpha Gene Polymorphisms and Endometriosis in An Iranian Population.
Babak Babaabasi, Ali Ahani, Faegheh Sadeghi, Haniyeh Bashizade-Fakhar, Hamid Reza Khorram Khorshid

Int J Fertil Steril· April 2019

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A soft computing approach for diabetes disease classification.
Mehrbakhsh Nilashi, Othman Bin Ibrahim, Abbas Mardani, Ali Ahani, Ahmad Jusoh

Health Informatics J· December 2018

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Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development.
Azadeh Shojaei, Reza Ebrahimzadeh-Vesal, Ali Ahani, Maryam Razzaghy-Azar, Golnaz Khakpour

Rep Biochem Mol Biol· October 2017

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Association study of the common polymorphisms in the folate-methionine pathway with retinoblastoma.
Elaheh Soleimani, Kioomars Saliminejad, Mohammad Taghi Akbari, Koorosh Kamali, Ali Ahani

Ophthalmic Genet· December 2016

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Accuracy Improvement for Predicting Parkinson's Disease Progression.
Mehrbakhsh Nilashi, Othman Ibrahim, Ali Ahani

Sci Rep· September 2016

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An Mutation (c.253dupC) Caused Diverse Phenotypes of Adrenoleukodystrophy in an Iranian Consanguineous Pedigree.
Masoud Mehrpour, Faeze Gohari, Majid Zaki Dizaji, Ali Ahani, May Christine V Malicdan

J Mol Genet Med· June 2016

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Methionine synthase A2756G variation is associated with the risk of retinoblastoma in Iranian children.
Mohammad Taghi Akbari, Asieh Naderi, Leila Saremi, Arezou Sayad, Shiva Irani, Ali Ahani

Cancer Epidemiol· December 2015

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Comparative evaluation of differentiation potential of menstrual blood- versus bone marrow-derived stem cells into hepatocyte-like cells.
Sayeh Khanjani, Manijeh Khanmohammadi, Amir-Hassan Zarnani, Mohammad-Mehdi Akhondi, Ali Ahani

PLoS One· November 2014

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Perspectives and editorials: letter to the editor.
Kioomars Saliminejad, Ali Ahani, Hamid Reza Khorram Khorshid

J Androl· October 2014

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Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification.
Fereshteh Ashtari, Kioomars Saliminejad, Ali Ahani, Koorosh Kamali, Zhamak Pahlevanzadeh

Avicenna J Med Biotechnol· October 2013

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Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification.
Ali Ahani, Mohammad Taghi Akbari, Kioomars Saliminejad, Babak Behnam, Mohammad Mehdi Akhondi

Mol Vis· September 2013

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Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome.
Babak Behnam, Marjan Shakiba, Ali Ahani, Maryam Razzaghy Azar

Hepat Mon· September 2013

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Rapid detection of RB1 recurrent mutations in retinoblastoma by ARMS-PCR.
Kioomars Saliminejad, Babak Behnam, Mohammad Taghi Akbari, Hamid Reza Khorram Khorshid, Farriba Ghassemi, Ali Ahani

J Genet· May 2013

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Genotyping of Polymorphic Microsatellite Markers Linked to RB1 Locus in Iranian Population.
Saman Mohamad Zahery, Kioomars Saliminejad, Hamid Reza Khorram Khorshid, Ali Ahani

Avicenna J Med Biotechnol· October 2012

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The role of IL-6 for predicting neonatal sepsis: a systematic review and meta-analysis.
Lobat Shahkar, Abbasali Keshtkar, Arezou Mirfazeli, Ali Ahani, Gholamreza Roshandel

Iran J Pediatr· December 2011

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RB1 gene mutations in Iranian patients with retinoblastoma: report of four novel mutations.
Ali Ahani, Babak Behnam, Hamid Reza Khorram Khorshid, Mohammad Taghi Akbari

Cancer Genet· June 2011

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Frequent loss of heterozygosity at 8p22 chromosomal region in diffuse type of gastric cancer.
Hedayat Allah Hosseini, Ali Ahani, Hamid Galehdari, Ali Mohammad Froughmand, Masoud Hosseini

World J Gastroenterol· June 2007

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